Variant #0000921834 (NC_000016.9:g.67198770C>A, NM_001374675.1:c.56C>A (HSF4))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.67198770C>A
DNA change (hg38) g.67164867C>A
Published as A20D
ISCN -
DB-ID HSF4_000002 See all 2 reported entries
Variant remarks markedly inhibited HSF4b oligomerization, inhibits transcription activation ability of HSF4b due to defective HSE-binding
Reference PubMed: Enoki 2010
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2023-03-21 19:18:05 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HSF4 NM_001374675.1 +/. - c.56C>A - p.Ala19Asp


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